Global Oncology Trials Leader - Senior

Alentis Therapeutics AG; Allschwil; On-site; CHF 180,000 - 260,000; Full time

Job summary

Alentis Therapeutics AG seeks a Senior Clinical Trial Leader Oncology to drive global clinical trials, acting as the face of the company to vendors and investigators. You will oversee cross-functional teams, ensure timelines, budgets, quality and regulatory compliance, and contribute to regulatory submissions.

The role requires strong leadership, strategic thinking, and extensive experience in oncology trials across multinational settings, with an emphasis on ICH-GCP and global development.

Qualifications

• Master's degree or equivalent university degree in Life Sciences, Healthcare, Pharmacy, or a related field.
• ≥8 years of clinical study management experience, including early-phase trials, preferably in biotech and global development environments.
• Strong understanding of oncology drug development and global clinical trial leadership.

Responsibilities

• Act as the primary Clinical Operations and/or Clinical Science lead for Alentis with external vendors and study partners.
• Lead and oversee preparation, execution, and delivery of complex global clinical trials within timelines, budgets, and quality standards.
• Provide strategic leadership for one or more studies and align across development programs.
• Coordinate development and review of study documents (protocols, ICFs, monitoring plans, SDSPs, CSRs) in line with SOPs and GCP.

Skills

Clinical trial leadership

Project management

Risk management

Vendor management

Cross-functional collaboration

Communication

Stakeholder management

Leadership

Regulatory knowledge

ICH-GCP

Education

Master's degree in Life Sciences

Job description

Alentis Therapeutics AG seeks a Senior Clinical Trial Leader Oncology to drive global clinical trials, acting as the face of the company to vendors and investigators. You will oversee cross-functional teams, ensure timelines, budgets, quality and regulatory compliance, and contribute to regulatory submissions.

The role requires strong leadership, strategic thinking, and extensive experience in oncology trials across multinational settings, with an emphasis on ICH-GCP and global development.